Drug intelligence / Profile preview

VT-109

Development stage
Preclinical
Lead developer
Vera Therapeutics
Modality
Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes
Administration
Intravenous
01

Overview

VT-109 is a novel, next-generation recombinant fusion protein designed to target and inhibit both B-cell activating factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), two members of the tumor necrosis factor ligand superfamily that play key roles in B cell survival, differentiation, and autoantibody production. Developed by Vera Therapeutics under license from Stanford University, VT-109 is engineered for enhanced potency, selectivity, or pharmacokinetic properties compared to earlier dual BAFF/APRIL inhibitors. Its primary mechanism involves blocking the activity of BAFF and APRIL to modulate B cell function in immunological diseases. Preclinical studies suggest broad therapeutic potential across a spectrum of B cell-mediated disorders[1][3][4][8][9].

Other names
VT 109VT109VT-109
02

Targets

TNFSF13 (APRIL)BAFF (Tumor necrosis factor ligand superfamily member 13B)

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